A COMPOUND HETEROZYGOUS MISSENSE MUTATION AND A LARGE DELETION IN THE KCTD7 GENE PRESENTING AS AN OPSOCLONUS-MYOCLONUS ATAXIA-LIKE SYNDROME

被引：0
|
作者：
Blumkin, L.
Kivity, S. [1 ]
Lev, D. [1 ]
Leshinsky-Silver, E. [1 ]
Lerman-Sagie, T. [1 ]
机构：
[1] Wolfson Med Ctr, Holon, Israel
来源：
EPILEPSIA | 2012年 / 53卷
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中图分类号：
R74 [神经病学与精神病学];
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页码：39 / 39
页数：1
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